Onur Emre Onat

1.2k total citations
18 papers, 792 citations indexed

About

Onur Emre Onat is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Onur Emre Onat has authored 18 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Onur Emre Onat's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Circadian rhythm and melatonin (2 papers) and Neurological disorders and treatments (2 papers). Onur Emre Onat is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Circadian rhythm and melatonin (2 papers) and Neurological disorders and treatments (2 papers). Onur Emre Onat collaborates with scholars based in Türkiye, United States and France. Onur Emre Onat's co-authors include Tayfun Özçelık, Ana C. Krieger, Scott S. Campbell, Michael W. Young, Alina Patke, Patricia Murphy, Süleyman Gülsüner, Meli̇ha Tan, Üner Tan and Haluk Topaloğlu and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Onur Emre Onat

18 papers receiving 773 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Onur Emre Onat Türkiye 11 311 241 173 121 117 18 792
Kimberly M. Newberry United States 13 681 2.2× 40 0.2× 236 1.4× 80 0.7× 58 0.5× 20 1.1k
Loredana Zocchi United States 12 327 1.1× 290 1.2× 83 0.5× 164 1.4× 89 0.8× 14 756
Laurence Borgs Belgium 12 304 1.0× 132 0.5× 43 0.2× 80 0.7× 100 0.9× 12 640
Leah Peleg Israel 14 270 0.9× 89 0.4× 181 1.0× 236 2.0× 75 0.6× 55 697
Romina Combi Italy 19 496 1.6× 54 0.2× 150 0.9× 97 0.8× 375 3.2× 38 1.1k
Michinori Koebis Japan 12 233 0.7× 65 0.3× 58 0.3× 34 0.3× 90 0.8× 31 427
Katherine L. Rosewell United States 18 123 0.4× 288 1.2× 318 1.8× 107 0.9× 146 1.2× 27 1.0k
Marie‐Paule Felder‐Schmittbuhl France 20 525 1.7× 522 2.2× 131 0.8× 144 1.2× 318 2.7× 45 1.1k
Ariane Sharif France 20 377 1.2× 249 1.0× 56 0.3× 127 1.0× 239 2.0× 40 1.0k
J. Kelly Ganjei United States 12 554 1.8× 87 0.4× 71 0.4× 577 4.8× 196 1.7× 14 1.2k

Countries citing papers authored by Onur Emre Onat

Since Specialization
Citations

This map shows the geographic impact of Onur Emre Onat's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Onur Emre Onat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Onur Emre Onat more than expected).

Fields of papers citing papers by Onur Emre Onat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Onur Emre Onat. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Onur Emre Onat. The network helps show where Onur Emre Onat may publish in the future.

Co-authorship network of co-authors of Onur Emre Onat

This figure shows the co-authorship network connecting the top 25 collaborators of Onur Emre Onat. A scholar is included among the top collaborators of Onur Emre Onat based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Onur Emre Onat. Onur Emre Onat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Schrodi, Steven J., Vinod Scaria, Onur Emre Onat, et al.. (2023). Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations. Genetics in Medicine Open. 2. 100840–100840. 1 indexed citations
2.
Onat, Onur Emre, et al.. (2023). Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosis. PeerJ. 11. e15250–e15250. 2 indexed citations
3.
Başak, A. Nazlı, Onur Emre Onat, Kaya Bilgüvar, et al.. (2021). The genetic structure of the Turkish population reveals high levels of variation and admixture. Proceedings of the National Academy of Sciences. 118(36). 47 indexed citations
4.
Onat, Onur Emre, Şeref Gül, Kaya Bilgüvar, et al.. (2020). Human CRY1 variants associate with attention deficit/hyperactivity disorder. Journal of Clinical Investigation. 130(7). 3885–3900. 33 indexed citations
5.
Güneş, Sezgin, et al.. (2020). Multiscale analysis of SRY‐positive 46,XX testicular disorder of sex development: Presentation of nine cases. Andrologia. 52(11). e13739–e13739. 6 indexed citations
6.
Onat, Onur Emre, Süleyman Gülsüner, Hilmi Uysal, et al.. (2018). Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation. Diagnostic and Interventional Radiology. 24(6). 392–401. 7 indexed citations
7.
Patke, Alina, Patricia Murphy, Onur Emre Onat, et al.. (2017). Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder. Cell. 169(2). 203–215.e13. 249 indexed citations
8.
Kanaan, Sami B., Onur Emre Onat, Nathalie Balandraud, et al.. (2016). Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis. PLoS ONE. 11(6). e0158550–e0158550. 25 indexed citations
9.
Ergüner, Bekir, Mahmut Şamil Sağıroğlu, Bayram Yüksel, et al.. (2014). Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair. Journal of Medical Genetics. 51(7). 455–459. 38 indexed citations
10.
Gülsüner, Süleyman, Onur Emre Onat, Tom Walsh, et al.. (2014). Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proceedings of the National Academy of Sciences. 111(51). 18285–18290. 92 indexed citations
11.
Güneş, Sezgin, et al.. (2013). Disruption ofHDXgene in premature ovarian failure. Systems Biology in Reproductive Medicine. 59(4). 218–222. 5 indexed citations
12.
Kanaan, Sami B., Onur Emre Onat, Nathalie Balandraud, et al.. (2013). A7.9 Does Telomere Shortening in Women with Rheumatoid Arthritis Predict X Chromosome Inactivation Bias?. Annals of the Rheumatic Diseases. 72. A51–A51. 1 indexed citations
13.
Onat, Onur Emre, Süleyman Gülsüner, Kaya Bilgüvar, et al.. (2012). Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. European Journal of Human Genetics. 21(3). 281–285. 100 indexed citations
14.
Güneş, Sezgin, Ramazan Aşçı, Onur Emre Onat, et al.. (2012). Two Males with SRY-Positive 46,XX Testicular Disorder of Sex Development. Systems Biology in Reproductive Medicine. 59(1). 42–47. 18 indexed citations
15.
Gülsüner, Süleyman, Ayşe B. Tekinay, Katja Doerschner, et al.. (2011). Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred. Genome Research. 21(12). 1995–2003. 51 indexed citations
16.
Onat, Onur Emre, Nathalie Balandraud, Sami B. Kanaan, et al.. (2011). Skewed X chromosome inactivation in rheumatoid arthritis women. Annals of the Rheumatic Diseases. 70. A88–A88. 1 indexed citations
17.
Özçelık, Tayfun, Nurten Akarsu, Elif Uz, et al.. (2008). Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans. Proceedings of the National Academy of Sciences. 105(11). 4232–4236. 71 indexed citations
18.
Onat, Onur Emre, Mesut Tez, Tayfun Özçelık, & Gökçe Törüner. (2006). MDM2 T309G polymorphism is associated with bladder cancer.. PubMed. 26(5A). 3473–5. 45 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kimberly M. Newberry Breakdown of academic impact, for papers by Loredana Zocchi Breakdown of academic impact, for papers by Laurence Borgs Breakdown of academic impact, for papers by Leah Peleg Breakdown of academic impact, for papers by Romina Combi Breakdown of academic impact, for papers by Michinori Koebis Breakdown of academic impact, for papers by Katherine L. Rosewell Breakdown of academic impact, for papers by Marie‐Paule Felder‐Schmittbuhl Breakdown of academic impact, for papers by Ariane Sharif Breakdown of academic impact, for papers by J. Kelly Ganjei
Rankless by CCL
2026